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Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy.
Al-Chalabi A, Dürr A, Wood NW, Parkinson MH, Camuzat A, Hulot JS, Morrison KE, Renton A, Sussmuth SD, Landwehrmeyer BG, Ludolph A, Agid Y, Brice A, Leigh PN, Bensimon G; NNIPPS Genetic Study Group. Al-Chalabi A, et al. Among authors: durr a. PLoS One. 2009 Sep 22;4(9):e7114. doi: 10.1371/journal.pone.0007114. PLoS One. 2009. PMID: 19771175 Free PMC article. Clinical Trial.
Genetics of movement disorders.
Dürr A, Brice A. Dürr A, et al. Curr Opin Neurol. 1996 Aug;9(4):290-7. doi: 10.1097/00019052-199608000-00009. Curr Opin Neurol. 1996. PMID: 8858187 Review.
Sequencing of the alpha-synuclein gene in a large series of cases of familial Parkinson's disease fails to reveal any further mutations. The European Consortium on Genetic Susceptibility in Parkinson's Disease (GSPD).
Vaughan JR, Farrer MJ, Wszolek ZK, Gasser T, Durr A, Agid Y, Bonifati V, DeMichele G, Volpe G, Lincoln S, Breteler M, Meco G, Brice A, Marsden CD, Hardy J, Wood NW. Vaughan JR, et al. Among authors: durr a. Hum Mol Genet. 1998 Apr;7(4):751-3. doi: 10.1093/hmg/7.4.751. Hum Mol Genet. 1998. PMID: 9499430
Genetic complexity and Parkinson's disease.
Gasser T, Müller-Myhsok B, Wszolek ZK, Dürr A, Vaughan JR, Bonifati V, Meco G, Bereznai B, Oehlmann R, Agid Y, Brice A, Wood N. Gasser T, et al. Among authors: durr a. Science. 1997 Jul 18;277(5324):388-9; author reply 389. Science. 1997. PMID: 9518367 No abstract available.
The alpha-synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: a study of 230 European cases. European Consortium on Genetic Susceptibility in Parkinson's Disease.
Vaughan J, Durr A, Tassin J, Bereznai B, Gasser T, Bonifati V, De Michele G, Fabrizio E, Volpe G, Bandmann O, Johnson WG, Golbe LI, Breteler M, Meco G, Agid Y, Brice A, Marsden CD, Wood NW. Vaughan J, et al. Among authors: durr a. Ann Neurol. 1998 Aug;44(2):270-3. doi: 10.1002/ana.410440221. Ann Neurol. 1998. PMID: 9708553
CYP2D6 polymorphism and Parkinson's disease susceptibility.
Sabbagh N, Brice A, Marez D, Dürr A, Legrand M, Lo Guidice JM, Destée A, Agid Y, Broly F. Sabbagh N, et al. Among authors: durr a. Mov Disord. 1999 Mar;14(2):230-6. doi: 10.1002/1531-8257(199903)14:2<230::aid-mds1005>3.0.co;2-6. Mov Disord. 1999. PMID: 10091614
[Genetics of Parkinson disease].
Brassat D, Durr A, Agid Y, Brice A. Brassat D, et al. Among authors: durr a. Rev Med Interne. 1999 Aug;20(8):709-14. doi: 10.1016/s0248-8663(99)80493-7. Rev Med Interne. 1999. PMID: 10480176 Review. French.
747 results